Yan Hai-Cheng, Wang Wei, Dou Chang-Wu, Tian Fu-Ming, Qi Song-Tao
Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Avenue North Road No. 1838, Guangzhou, 510515, People's Republic of China.
Mol Biol Rep. 2014 Jul;41(7):4425-34. doi: 10.1007/s11033-014-3313-4. Epub 2014 Mar 5.
This meta-analysis was undertaken to identify the relationships between genetic polymorphisms in the LDLR gene and the risk of cerebral infarction. The Web of Science (1945-2013), the Cochrane Library Database (Issue 12, 2013), PubMed (1966-2013), EMBASE (1980-2013), CINAHL (1982-2013) and the Chinese Biomedical Database (CBM) (1982-2013) were searched for relevant articles without language restrictions. Meta-analysis was conducted using the STATA 12.0 software. Crude odds ratios (OR) with their corresponding 95% confidence interval (CI) were calculated. Eight case-control studies with a total of 4,655 patients with cerebral infarction and 15,920 healthy control subjects were included in our meta-analysis. Five common polymorphisms in the LDLR gene were evaluated, including rs11669576 A > T, rs1433099 C > T, rs5925 C > T, rs688 C > T, rs1122608 T > G in the LDLR gene. The results of this meta-analysis revealed that cerebral infarction patients had a higher frequency of LDLR genetic polymorphisms than that of healthy controls (allele model: OR 1.17, 95% CI 1.05-1.30, P = 0.004; dominant model: OR 1.18, 95% CI 1.05-1.33, P = 0.007; homozygous model: OR 1.50, 95% CI 1.03-2.16, P = 0.032; respectively), especially for the rs11669576 A > T, rs1433099 C > T and rs5925 C > T polymorphisms. Among different ethnic subgroups, the results demonstrated positive correlations between LDLR genetic polymorphisms and an increased risk of cerebral infarction among both Asians and Caucasians under the allele and dominant models (all P < 0.05). Our findings indicate that LDLR genetic polymorphisms may be strongly involved in the pathogenesis of cerebral infarction, especially the rs11669576 A > T, rs1433099 C > T, rs5925 C > T polymorphisms.
本荟萃分析旨在确定低密度脂蛋白受体(LDLR)基因多态性与脑梗死风险之间的关系。检索了科学网(1945 - 2013年)、考克兰图书馆数据库(2013年第12期)、PubMed(1966 - 2013年)、EMBASE(1980 - 2013年)、护理学与健康领域数据库(CINAHL,1982 - 2013年)以及中国生物医学文献数据库(CBM,1982 - 2013年),以查找无语言限制的相关文章。使用STATA 12.0软件进行荟萃分析。计算了粗比值比(OR)及其相应的95%置信区间(CI)。我们的荟萃分析纳入了8项病例对照研究,共4655例脑梗死患者和15920例健康对照者。评估了LDLR基因中的5种常见多态性,包括LDLR基因中的rs11669576 A>T、rs1433099 C>T、rs5925 C>T、rs688 C>T、rs1122608 T>G。该荟萃分析结果显示,脑梗死患者LDLR基因多态性的频率高于健康对照者(等位基因模型:OR 1.17,95%CI 1.05 - 1.30,P = 0.004;显性模型:OR 1.18,95%CI 1.05 - 1.33,P = 0.007;纯合子模型:OR 1.50,95%CI 1.03 - 2.16,P = 0.032;分别),尤其是rs11669576 A>T、rs1433099 C>T和rs5925 C>T多态性。在不同种族亚组中,结果表明在等位基因和显性模型下,亚洲人和高加索人中LDLR基因多态性与脑梗死风险增加之间均存在正相关(所有P<0.05)。我们的研究结果表明,LDLR基因多态性可能在脑梗死的发病机制中起重要作用,尤其是rs11669576 A>T、rs1433099 C>T、rs5925 C>T多态性。